Drug-induced alterations in Mg2+ homoeostasis

被引:50
作者
Lameris, Anke L. [1 ]
Monnens, Leo A. [1 ]
Bindels, Rene J. [1 ]
Hoenderop, Joost G. J. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Physiol, NL-6500 HB Nijmegen, Netherlands
关键词
drug induction; hypermagnesaemia; hypomagnesaemia; ion channel; kidney; magnesium; PROTON-PUMP INHIBITORS; THICK ASCENDING LIMB; RENAL MAGNESIUM LOSS; RAT TUBULAR FLUID; SEVERE HYPERMAGNESEMIA; EPSOM SALT; INTRACELLULAR MAGNESIUM; SEVERE HYPOMAGNESEMIA; CONVOLUTED TUBULE; MISSENSE MUTATION;
D O I
10.1042/CS20120045
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Magnesium (Mg2+) balance is tightly regulated by the concerted actions of the intestine, bone and kidneys. This balance can be disturbed by a broad variety of drugs. Diuretics, modulators of the EGFR (epidermal growth factor receptor), proton pump inhibitors, antimicrobials, calcineurin inhibitors and cytostatics may all cause hypomagnesaemia, potentially leading to tetany, seizures and cardiac arrhythmias. Conversely, high doses of Mg2+ salts, frequently administered as an antacid or a laxative, may lead to hypermagnesaemia causing various cardiovascular and neuromuscular abnormalities. A better understanding of the molecular mechanisms underlying the adverse effects of these medications on Mg2+ balance will indicate ways of prevention and treatment of these adverse effects and could potentially provide more insight into Mg2+ homoeostasis.
引用
收藏
页码:1 / 14
页数:14
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